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@ARTICLE{Pham:202145,
      author       = {Pham, Cong-Dat and Hartmann, Rudolf and Böhler, Philip and
                      Stork, Björn and Wesselborg, Sebastian and Lin, Wenhan and
                      Lai, Daowan and Proksch, Peter},
      title        = {{C}allyspongiolide, a {C}ytotoxic {M}acrolide from the
                      {M}arine {S}ponge {C}allyspongia sp.},
      journal      = {Organic letters},
      volume       = {16},
      number       = {1},
      issn         = {1523-7052},
      address      = {Washington, DC},
      publisher    = {ACS},
      reportid     = {FZJ-2015-04434},
      pages        = {266 - 269},
      year         = {2014},
      abstract     = {A novel macrolide, callyspongiolide, whose structure was
                      determined by comprehensive analysis of the NMR and HRMS
                      spectra, was isolated from the marine sponge Callyspongia
                      sp. collected in Indonesia. The compound features a
                      carbamate-substituted 14-membered macrocyclic lactone ring
                      with a conjugated structurally unprecedented diene-ynic side
                      chain terminating at a brominated benzene ring.
                      Callyspongiolide showed strong cytotoxicity against human
                      Jurkat J16 T and Ramos B lymphocytes.},
      cin          = {ICS-6},
      ddc          = {540},
      cid          = {I:(DE-Juel1)ICS-6-20110106},
      pnm          = {452 - Structural Biology (POF2-452)},
      pid          = {G:(DE-HGF)POF2-452},
      typ          = {PUB:(DE-HGF)16},
      UT           = {WOS:000329472800069},
      pubmed       = {pmid:24329175},
      doi          = {10.1021/ol403241v},
      url          = {https://juser.fz-juelich.de/record/202145},
}